Principal Scientific Writer at Novartis

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

22 Feb, 26

Salary

0.0

Posted On

24 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary To write, support, manage and provide consultancy to senior and expert scientific writers to prepare all high quality medical and scientific communications including literature review, abstracts, posters, slide decks, Manuscripts (complex) for publication/ presentation. Job Description Principal Scientific Writer Location – Hyderabad #LI Hybrid Major Responsibilities: Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques. Manages multiple projects across multiple brands and therapeutic areas. Defines and implements stakeholder management strategies and tactics. Develops a Center of Excellence (CoE) for identified TA/disease area/deliverable. Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion. Ideates and implements tactics to influence internal and external development environment. Complies with and support group’s project management tool, standards, policies and initiatives. Follows Novartis specifications for documentation, templates etc. Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance. Trains new joiners, fellow colleagues as and when required. Performs additional tasks as assigned. Minimum Requirements: Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M. Pharm +10 years of clinical research (CR) experience. Desired: Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) PhD > 8 year of CR experience, MBBS/equivalent >8 year of CR experience, MD >6 years of CR exp Key Performance Indicators Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. complying with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc). Drive maximum efficiency from the teams working on projects assigned. Publications are acceptable to internal and external authors (no issues with authorship). Completion of an adequate number of medical and scientific documents (taking into account complexity) per year. Active contribution to knowledge creation, use and dissemination activities. Adheres to Novartis values and behaviors. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Skills Desired Agility, Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care, People Management, Pharmaceutics, Priority Disease Areas Expertise, Product Launches, Product Strategy, Real World Evidence (RWE), Regulatory Compliance, Research Methodologies {+ 3 more} Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The Principal Scientific Writer prepares and supports the preparation of highly complex scientific documents to meet the highest quality standards. They manage multiple projects across various brands and therapeutic areas while providing strategic inputs to development and brand plans.